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FXN gene methylation determines carrier status in Friedreich ataxia

Authors

  • Christina Lam Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA PubMed articlesGoogle scholar articles
  • Kaitlyn M Gilliam Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA PubMed articlesGoogle scholar articles
  • Layne N Rodden Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA PubMed articlesGoogle scholar articles
  • Kimberly A Schadt Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA PubMed articlesGoogle scholar articles
  • David R Lynch Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA PubMed articlesGoogle scholar articles
  • Sanjay Bidichandani Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA Department of Biochemistry & Molecular Biology, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Sanjay Bidichandani, Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA; sanjay-bidichandani{at}ouhsc.edu
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Citation

Lam C, Gilliam KM, Rodden LN, et al
FXN gene methylation determines carrier status in Friedreich ataxia

Publication history

  • Received June 3, 2022
  • Accepted January 4, 2023
  • First published January 12, 2023.
Online issue publication 
July 21, 2023

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